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A unique cytotoxic CD4+ T cell-signature defines critical COVID-19
Clinical & Translational Immunology ( IF 5.8 ) Pub Date : 2023-08-28 , DOI: 10.1002/cti2.1463
Sarah Baird 1, 2 , Caroline L Ashley 1, 2 , Felix Marsh-Wakefield 2, 3, 4 , Sibel Alca 1, 2 , Thomas M Ashhurst 2, 5 , Angela L Ferguson 2, 3 , Hannah Lukeman 1, 2 , Claudio Counoupas 1, 2, 6 , Jeffrey J Post 7, 8 , Pamela Konecny 7, 9 , Adam Bartlett 10, 11, 12 , Marianne Martinello 10 , Rowena A Bull 10, 11 , Andrew Lloyd 10, 11 , Alice Grey 13 , Owen Hutchings 13 , Umaimainthan Palendira 2, 3 , Warwick J Britton 6, 14 , Megan Steain 1, 2 , James A Triccas 1, 2
Affiliation  

SARS-CoV-2 infection causes a spectrum of clinical disease presentation, ranging from asymptomatic to fatal. While neutralising antibody (NAb) responses correlate with protection against symptomatic and severe infection, the contribution of the T-cell response to disease resolution or progression is still unclear. As newly emerging variants of concern have the capacity to partially escape NAb responses, defining the contribution of individual T-cell subsets to disease outcome is imperative to inform the development of next-generation COVID-19 vaccines.

中文翻译:

独特的细胞毒性 CD4+ T 细胞特征定义了关键的 COVID-19

SARS-CoV-2 感染会导致一系列临床疾病表现,从无症状到致命。虽然中和抗体 (NAb) 反应与针对症状和严重感染的保护相关,但 T 细胞反应对疾病消退或进展的贡献仍不清楚。由于新出现的令人关注的变体有能力部分逃避 NAb 反应,因此确定个体 T 细胞亚群对疾病结果的贡献对于下一代 COVID-19 疫苗的开发至关重要。
更新日期:2023-08-29
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